Skip to main content

Probing the Plasma Membrane Structure of Immune Cells Through the Analysis of Membrane Sheets by Electron Microscopy

  • Protocol
  • First Online:
Book cover Immune Receptors

Part of the book series: Methods in Molecular Biology ((MIMB,volume 748))

Abstract

This chapter describes a method to generate plasma membrane sheets that are large enough to visualize the membrane architecture and perform quantitative analyses of protein distributions. This procedure places the sheets on electron microscopy grids, parallel to the imaging plane of the microscope, where they can be characterized by transmission electron microscopy. The basic principle of the technique is that cells are broken open (“ripped”) through mechanical forces applied by the separation of two opposing surfaces sandwiching the cell, with one of the surfaces coated onto an EM grid. The exposed inner membrane surfaces can then be visualized with electron dense stains and specific proteins can be detected with gold conjugated probes.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 159.00
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 109.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Singer SJ, Nicolson GL. (1972) The fluid mosaic model of the structure of cell membranes. Science 175 (23):720–31.

    Article  PubMed  CAS  Google Scholar 

  2. van Meer G, Simons K. (1982) Viruses budding from either the apical or the basolateral plasma membrane domain of MDCK cells have unique phospholipid compositions. Embo J 1 (7):847–52.

    PubMed  Google Scholar 

  3. Sako Y, Kusumi A. (1994) Compartmentalized structure of the plasma membrane for receptor movements as revealed by a nanometer-level motion analysis. J Cell Biol 125 (6):1251–64.

    Article  PubMed  CAS  Google Scholar 

  4. Lillemeier BF, Pfeiffer JR, Surviladze Z, Wilson BS, Davis MM. (2006) Plasma membrane-associated proteins are clustered into islands attached to the cytoskeleton. Proc Natl Acad Sci USA 103 (50):18992–7.

    Article  PubMed  CAS  Google Scholar 

  5. Monks CR, Freiberg BA, Kupfer H, Sciaky N, Kupfer A. (1998) Three-dimensional segregation of supramolecular activation clusters in T cells. Nature 395 (6697):82–6.

    Article  PubMed  CAS  Google Scholar 

  6. Sanan DA, Anderson RG. (1991) Simultaneous visualization of LDL receptor distribution and clathrin lattices on membranes torn from the upper surface of cultured cells. J Histochem Cytochem 39 (8):1017–24.

    Article  PubMed  CAS  Google Scholar 

  7. Lillemeier BF, Mortelmaier MA, Forstner MB, Huppa JB, Groves JT, Davis MM. (2010) TCR and Lat are expressed on separate protein islands on T cell membranes and concatenate during activation. Nat Immunol 11 (1):90–6.

    Article  PubMed  CAS  Google Scholar 

  8. Kim JH, Cramer L, Mueller H, Wilson B, Vilen BJ. (2005) Independent Trafficking of Ig-{alpha}/Ig-{beta} and {micro}-Heavy Chain Is Facilitated by Dissociation of the B Cell Antigen Receptor Complex. J Immunol 175 (1):147–54.

    PubMed  CAS  Google Scholar 

  9. Wilson BS, Pfeiffer JR, Oliver JM. (2000) Observing FcepsilonRI signaling from the inside of the mast cell membrane. J Cell Biol 149 (5):1131–42.

    Article  PubMed  CAS  Google Scholar 

  10. Wilson BS, Pfeiffer JR, Surviladze Z, Gaudet EA, Oliver JM. (2001) High resolution mapping of mast cell membranes reveals primary and secondary domains of Fc(epsilon)RI and LAT. J Cell Biol 154 (3):645–58.

    Article  PubMed  CAS  Google Scholar 

  11. Prior IA, Muncke C, Parton RG, Hancock JF. (2003) Direct visualization of Ras proteins in spatially distinct cell surface microdomains. J Cell Biol 160 (2):165–70.

    Article  PubMed  CAS  Google Scholar 

  12. Morone N, Fujiwara T, Murase K, et al. (2006) Three-dimensional reconstruction of the membrane skeleton at the plasma membrane interface by electron tomography. J Cell Biol 174 (6):851–62.

    Article  PubMed  CAS  Google Scholar 

  13. Ripley BD. (1977) Modeling spatial patterns. J. R. Stat. Soc. B39:172–212.

    Google Scholar 

  14. Zhang J, Leiderman K, Pfeiffer JR, Wilson BS, Oliver JM, Steinberg SL. (2006) Characterizing the topography of membrane receptors and signaling molecules from spatial patterns obtained using nanometer-scale electron-dense probes and electron microscopy. Micron 37 (1):14–34.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

The authors thank Dr. Bridget S. Wilson for advice on TEM and plasma membrane sheet preparation, and Dr. Fleur E. Tynan for comments on the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mark M. Davis .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2011 Springer Science+Business Media, LLC

About this protocol

Cite this protocol

Lillemeier, B.F., Davis, M.M. (2011). Probing the Plasma Membrane Structure of Immune Cells Through the Analysis of Membrane Sheets by Electron Microscopy. In: Rast, J., Booth, J. (eds) Immune Receptors. Methods in Molecular Biology, vol 748. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-61779-139-0_12

Download citation

  • DOI: https://doi.org/10.1007/978-1-61779-139-0_12

  • Published:

  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-61779-138-3

  • Online ISBN: 978-1-61779-139-0

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics